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High expression of DEK predicts poor prognosis of gastric adenocarcinoma
BACKGROUND: DEK, as an oncoprotein, plays an important role in cancer development and progression. This study aimed to investigate the clinicopathological significance of DEK overexpression in patients with gastric cancer. MATERIALS AND METHODS: The expression of DEK protein was evaluated by immunoh...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3994479/ https://www.ncbi.nlm.nih.gov/pubmed/24650035 http://dx.doi.org/10.1186/1746-1596-9-67 |
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author | Piao, Junjie Shang, Yongjun Liu, Shuangping Piao, Yingshi Cui, Xuelian Li, Yuzi Lin, Zhenhua |
author_facet | Piao, Junjie Shang, Yongjun Liu, Shuangping Piao, Yingshi Cui, Xuelian Li, Yuzi Lin, Zhenhua |
author_sort | Piao, Junjie |
collection | PubMed |
description | BACKGROUND: DEK, as an oncoprotein, plays an important role in cancer development and progression. This study aimed to investigate the clinicopathological significance of DEK overexpression in patients with gastric cancer. MATERIALS AND METHODS: The expression of DEK protein was evaluated by immunohistochemical (IHC) staining of 172 gastric cancer samples with complete clinicopathological features, and the correlation between DEK expression and clinicopathological features was examined. Survival rates were also calculated using the Kaplan-Meier method in gastric cancer patients with complete survival data. RESULTS: DEK protein showed a strictly nuclear staining pattern in gastric cancers with IHC and immunofluorescence. The strongly positive rate of DEK protein was 60.5% (104/172) in gastric cancers, which was significantly higher than that in either gastric dysplasia (19.4%, 7/36) or adjacent normal mucosa (0%, 0/27). DEK expression in gastric cancer correlated to tumor size, differentiation, clinical stage, disease-free survival, and overall survival rates. Further analysis showed that patients with early-stage gastric cancer and high DEK expression had shorter disease-free survival and overall survival duration than those with low DEK expression. CONCLUSION: High level of DEK protein expression predicts the poor prognosis of patients with gastric cancer. DEK expression might be potentially used as an independent effective biomarker for prognostic evaluation of gastric cancers. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/5050145571193097 |
format | Online Article Text |
id | pubmed-3994479 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-39944792014-04-23 High expression of DEK predicts poor prognosis of gastric adenocarcinoma Piao, Junjie Shang, Yongjun Liu, Shuangping Piao, Yingshi Cui, Xuelian Li, Yuzi Lin, Zhenhua Diagn Pathol Research BACKGROUND: DEK, as an oncoprotein, plays an important role in cancer development and progression. This study aimed to investigate the clinicopathological significance of DEK overexpression in patients with gastric cancer. MATERIALS AND METHODS: The expression of DEK protein was evaluated by immunohistochemical (IHC) staining of 172 gastric cancer samples with complete clinicopathological features, and the correlation between DEK expression and clinicopathological features was examined. Survival rates were also calculated using the Kaplan-Meier method in gastric cancer patients with complete survival data. RESULTS: DEK protein showed a strictly nuclear staining pattern in gastric cancers with IHC and immunofluorescence. The strongly positive rate of DEK protein was 60.5% (104/172) in gastric cancers, which was significantly higher than that in either gastric dysplasia (19.4%, 7/36) or adjacent normal mucosa (0%, 0/27). DEK expression in gastric cancer correlated to tumor size, differentiation, clinical stage, disease-free survival, and overall survival rates. Further analysis showed that patients with early-stage gastric cancer and high DEK expression had shorter disease-free survival and overall survival duration than those with low DEK expression. CONCLUSION: High level of DEK protein expression predicts the poor prognosis of patients with gastric cancer. DEK expression might be potentially used as an independent effective biomarker for prognostic evaluation of gastric cancers. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/5050145571193097 BioMed Central 2014-03-20 /pmc/articles/PMC3994479/ /pubmed/24650035 http://dx.doi.org/10.1186/1746-1596-9-67 Text en Copyright © 2014 Piao et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Piao, Junjie Shang, Yongjun Liu, Shuangping Piao, Yingshi Cui, Xuelian Li, Yuzi Lin, Zhenhua High expression of DEK predicts poor prognosis of gastric adenocarcinoma |
title | High expression of DEK predicts poor prognosis of gastric adenocarcinoma |
title_full | High expression of DEK predicts poor prognosis of gastric adenocarcinoma |
title_fullStr | High expression of DEK predicts poor prognosis of gastric adenocarcinoma |
title_full_unstemmed | High expression of DEK predicts poor prognosis of gastric adenocarcinoma |
title_short | High expression of DEK predicts poor prognosis of gastric adenocarcinoma |
title_sort | high expression of dek predicts poor prognosis of gastric adenocarcinoma |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3994479/ https://www.ncbi.nlm.nih.gov/pubmed/24650035 http://dx.doi.org/10.1186/1746-1596-9-67 |
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